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Titlebook: Bioinformatics; An Introductory Text Thomas Dandekar,Meik Kunz Book 20231st edition Springer-Verlag GmbH Germany, part of Springer Nature 2

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https://doi.org/10.1007/978-3-662-25516-2r complex calculations. The nanocellulose chip is potentially superior to today’s computer chips. It uses DNA for storage and light-controlled polymerases and exonucleases for reading in and out the stored information. Modulating proteins and processes act electronically across the nanocellulose mem
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https://doi.org/10.1007/978-3-662-25516-2ex properties (“feature extraction“), pattern recognition from large amounts of data (“training data set”) and then also for individual molecules or sequences (predictions, for example, for the secondary structure in the protein, for the localisation in the cell, etc.).
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How to Promote the Morphological Sciencesin-protein interactions and signalling cascades involved. Brain blueprints, so-called connectomes, are already available for . and are being intensively developed for other model organisms and humans. Numerous special software are available for clinical evaluations (EEG, computer tomograms) (‘medica
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Sequence Analysis: Deciphering the Language of LifeBLAST) and domain databases (Pfam, SMART). Crucial is the ability to know and use such software on the web, the tutorials and exercises encourage this. Programming sequence comparison software and databases only makes sense if it enables a better analysis of the biological question, in particular fo
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Magic RNAlls and the CRISPR/Cas9 system from bacteria underline the importance of RNA for molecular biology. Typically, one analyzes RNA sequence, structure, and folding energy orientationally first using RNAAnalyzer software, Rfam database, and RNAfold server. GEO and GeneVestigator databases show gene expr
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Genomes: Molecular Maps of Living Organismsst cell genome were completely sequenced and bioinformatically analysed in the 1990s, human genomes and numerous other eukaryotic (cells with a cell nucleus) genomes followed from 2001. The function of individual genes is identified by sequence comparisons: Protein function analysis (see Chap. .), b
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Modeling Metabolism and Finding New Antibioticslved. It is then possible to calculate which metabolic pathways and enzyme chains keep the metabolites in a network in equilibrium (flux balance analysis), which of these are also no longer decomposable (elementary mode analysis) and which of these are sufficient to represent all real metabolic situ
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